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5-Fluoro-DET

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(Redirected from 5F-DET) Chemical compound

Pharmaceutical compound
5-Fluoro-DET
Clinical data
Other names
  • 5-F-DET
  • 5-Fluoro-N,N-diethyltryptamine
Identifiers
IUPAC name
  • N,N-diethyl-2-(5-fluoro-1H-indol-3-yl)ethanamine
PubChem CID
ChemSpider
ChEMBL
Chemical and physical data
FormulaC14H19FN2
Molar mass234.318 g·mol
3D model (JSmol)
SMILES
  • CCN(CC)CCC1=CNC2=C1C=C(C=C2)F
InChI
  • InChI=1S/C14H19FN2/c1-3-17(4-2)8-7-11-10-16-14-6-5-12(15)9-13(11)14/h5-6,9-10,16H,3-4,7-8H2,1-2H3
  • Key:LBJIPBJDJFZKIQ-UHFFFAOYSA-N

5-Fluoro-DET (5F-DET, 5-fluoro-N,N-diethyltryptamine) is a tryptamine derivative related to drugs such as DET and 5-MeO-DET. It acts as an inhibitor of the enzyme myeloperoxidase, and is also thought to be an agonist at the 5-HT2A receptor.

See also

References

  1. Pelchowicz Z, Kaluszyner A, Bentov M (1961). "1067. N-alkylated 5-fluorotryptamines". Journal of the Chemical Society (Resumed): 5418–5421. doi:10.1039/JR9610005418.
  2. Kalir A, Szara S (May 1966). "Synthesis and pharmacological activity of alkylated tryptamines". Journal of Medicinal Chemistry. 9 (3): 341–4. doi:10.1021/jm00321a017. PMID 5960901.
  3. Soubhye J, Prévost M, Van Antwerpen P, Zouaoui Boudjeltia K, Rousseau A, Furtmüller PG, Obinger C, Vanhaeverbeek M, Ducobu J, Néve J, Gelbcke M, Dufrasne FO (December 2010). "Structure-based design, synthesis, and pharmacological evaluation of 3-(aminoalkyl)-5-fluoroindoles as myeloperoxidase inhibitors" (PDF). Journal of Medicinal Chemistry. 53 (24): 8747–59. doi:10.1021/jm1009988. PMID 21090682. S2CID 207225972.
  4. WO 2021/168082, Kruegel AC, Sporn J, "Specific Tryptamines for use in the Treatment of Mood Disorders.", published 26 August 2021, assigned to Gilgamesh Pharmaceuticals, Inc.. 
Tryptamines
Tryptamines
N-Acetyltryptamines
α-Alkyltryptamines
Triptans
Cyclized tryptamines
Isotryptamines
Related compounds
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